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Protein Function Development Team Leader
Protein Function Development Team Leader
EMBL-EBI
Hinxton, Saffron Walden (CB10), CB10 1SA
From £89,499 to £114,027 per annum
Overview - We are seeking an exceptional candidate for the EMBL-EBI Faculty role of Protein Function Development Team Leader, to be responsible for leading the engineering and bioinformatics infrastructure that underpins one of the most important resources in the life sciences, Uniprot. UniProt is the world's leading resource for protein sequences and functional annotation, used by hundreds of thousands of researchers globally every day. It provides comprehensive annotations across an ever-growing number of proteomes spanning the tree of life, integrating experimentally determined functional data from the literature with state-of-the-art computational predictions and richly interconnected data from partner resources. As the demands on UniProt continue to grow, in data volume, annotation depth, and the diversity of research applications it supports, a robust and ...
Overview - We are seeking an exceptional candidate for the EMBL-EBI Faculty role of Protein Function Development Team Leader, to be responsible for leading the engineering and bioinformatics infrastructure that underpins one of the most important resources in the life sciences, Uniprot. UniProt is the world's leading resource for protein sequences and functional annotation, used by hundreds of thousands of researchers globally every day. It provides comprehensive annotations across an ever-growing number of proteomes spanning the tree of life, integrating experimentally determined functional data from the literature with state-of-the-art computational predictions and richly interconnected data from partner resources. As the demands on UniProt continue to grow, in data volume, annotation depth, and the diversity of research applications it supports, a robust and ...
NEWPREMIUM
Google Measurement Protocol & other server-side API technologies.
Google Measurement Protocol & other server-side API technologies.
Familiarity with database management tools and techniques (e.g., SQL, Selenium, S3, Sagemaker, API protocols) is preferred but not required.
Familiarity with database management tools and techniques (e.g., SQL, Selenium, S3, Sagemaker, API protocols) is preferred but not required.
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Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in Endocrinology / Metabolic related areas, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in Endocrinology / Metabolic related areas, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
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The Medical Affairs Director UK is a key member of the Country DPS Board, acting as a strategic partner to the business. Medical Affairs Group Medical Affairs * Collaborate with Global Franchise Medical Affairs teams to shape the global innovation agenda through customer insights and identification of unmet needs. * Experience in research and/or industry roles (Medical Affairs, Clinical, or R&D) within a highly regulated pharmaceutical or medical device environment. Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Consulting, Customer Analytics, Design Mindset, Digital Culture, Digital Literacy, Healthcare Trends, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Product Strategies, Strategic Thinking, Tactical Thinking, Technical Credibility * Build and maintain strong external relationships with key stakeholders, including ...
The Medical Affairs Director UK is a key member of the Country DPS Board, acting as a strategic partner to the business. Medical Affairs Group Medical Affairs * Collaborate with Global Franchise Medical Affairs teams to shape the global innovation agenda through customer insights and identification of unmet needs. * Experience in research and/or industry roles (Medical Affairs, Clinical, or R&D) within a highly regulated pharmaceutical or medical device environment. Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Consulting, Customer Analytics, Design Mindset, Digital Culture, Digital Literacy, Healthcare Trends, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Product Strategies, Strategic Thinking, Tactical Thinking, Technical Credibility * Build and maintain strong external relationships with key stakeholders, including ...
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Clinical Trial Managers with expertise in Oncology or other therapy areas are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in Stirling, UK. * Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables * Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred; We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates. Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary
Clinical Trial Managers with expertise in Oncology or other therapy areas are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in Stirling, UK. * Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables * Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred; We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates. Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary
InterPro/Pfam Software Project Leader
InterPro/Pfam Software Project Leader
EMBL-EBI
Hinxton, Saffron Walden (CB10), CB10 1SA
From £57,520 to £77,212 per annum
We are seeking to hire an InterPro/Pfam Software Project leader to lead a cultural and technical shift towards AI-first development, leveraging AI coding assistants and generative tools to accelerate delivery, improve code quality, and reduce technical debt across both platforms. In your role, you will lead the software development team responsible for the Pfam and InterPro databases. Reporting to the Head of the Protein Families Group at EMBL-EBI, this role sits at the intersection of cutting-edge bioinformatics and modern software engineering. The team currently comprises of several software developers and engineers. * Lead the Pfam/InterPro software development team, managing workload, priorities, and professional development. * Drive the transition to AI-first software development practices, embedding AI coding tools (e.g. Claude Code, GitHub Copilot) into production workflows.
We are seeking to hire an InterPro/Pfam Software Project leader to lead a cultural and technical shift towards AI-first development, leveraging AI coding assistants and generative tools to accelerate delivery, improve code quality, and reduce technical debt across both platforms. In your role, you will lead the software development team responsible for the Pfam and InterPro databases. Reporting to the Head of the Protein Families Group at EMBL-EBI, this role sits at the intersection of cutting-edge bioinformatics and modern software engineering. The team currently comprises of several software developers and engineers. * Lead the Pfam/InterPro software development team, managing workload, priorities, and professional development. * Drive the transition to AI-first software development practices, embedding AI coding tools (e.g. Claude Code, GitHub Copilot) into production workflows.
PREMIUM
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Director, Regional Ecosystem Lead (Northern Europe & UK)
Director, Regional Ecosystem Lead (Northern Europe & UK)
CSL Behring
Fishery, Maidenhead (SL6), SL6 1PT
Competitive
Could you be our next Director, Regional Ecosystem Lead (Northern Europe & UK). Partner closely with TA Search Leads to conduct regional searches, plan engagements and conferences, and share regional insights and updates.? Serve as the key CSL leader within the regional innovation ecosystem, actively sourcing opportunities aligned with all TA strategies and portfolio priorities. Serve as a senior member of deal teams occurring in each region, supporting transactions from identification through due diligence and help lead relationships with external partners through deal close.? Provide insights on regional biotech trends, competitive landscape, and innovation hotspots. 10+ years in biopharma, external innovation, or business development with strong regional network and ecosystem knowledge.? Proven ability to source and evaluate external opportunities and lead deal execution.?
Could you be our next Director, Regional Ecosystem Lead (Northern Europe & UK). Partner closely with TA Search Leads to conduct regional searches, plan engagements and conferences, and share regional insights and updates.? Serve as the key CSL leader within the regional innovation ecosystem, actively sourcing opportunities aligned with all TA strategies and portfolio priorities. Serve as a senior member of deal teams occurring in each region, supporting transactions from identification through due diligence and help lead relationships with external partners through deal close.? Provide insights on regional biotech trends, competitive landscape, and innovation hotspots. 10+ years in biopharma, external innovation, or business development with strong regional network and ecosystem knowledge.? Proven ability to source and evaluate external opportunities and lead deal execution.?
The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. We are seeking several Medical Directors to join our dynamic team. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Coordinate with other departments in all phases of the studies and trials including feasibility ...
The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. We are seeking several Medical Directors to join our dynamic team. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Coordinate with other departments in all phases of the studies and trials including feasibility ...
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We're seeking aProject Managero help us take vision to value and create lasting impact for one of our life sciences managed accounts - As the Project Manager, you will lead the end-to-end delivery of a confidential project scheduled to go live on July 1, 2027. * 10+ years of experience as a Project Manager, with a strong understanding of data and analytics, finance, and legal knowledge - You will develop and manage comprehensive project plans, coordinate internal and external teams, and oversee risk and issue management. Additionally, you will engage stakeholders, ensure quality and governance throughout the project lifecycle, and manage meetings, communications, and documentation across multiple business functions and third-party stakeholders * Develop and manage comprehensive project plans to ensure the successful delivery of the confidential project
We're seeking aProject Managero help us take vision to value and create lasting impact for one of our life sciences managed accounts - As the Project Manager, you will lead the end-to-end delivery of a confidential project scheduled to go live on July 1, 2027. * 10+ years of experience as a Project Manager, with a strong understanding of data and analytics, finance, and legal knowledge - You will develop and manage comprehensive project plans, coordinate internal and external teams, and oversee risk and issue management. Additionally, you will engage stakeholders, ensure quality and governance throughout the project lifecycle, and manage meetings, communications, and documentation across multiple business functions and third-party stakeholders * Develop and manage comprehensive project plans to ensure the successful delivery of the confidential project
We are seeking a Hematologist Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. **All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts;
We are seeking a Hematologist Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. **All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts;
Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our analysts work directly with Clinical Operation teams to identify needs and establish solutions spanning data analytics, visualization, and accessibility. Analysts will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency. Analysts will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering team. * Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and * Bachelors in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; * Clinical research experience is preferred;
Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our analysts work directly with Clinical Operation teams to identify needs and establish solutions spanning data analytics, visualization, and accessibility. Analysts will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency. Analysts will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering team. * Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and * Bachelors in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; * Clinical research experience is preferred;
Medpace is currently seeking candidates with Oncology PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical ...
Medpace is currently seeking candidates with Oncology PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical ...
We are seeking an Oncologist - Solid Tumor Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. **All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts;
We are seeking an Oncologist - Solid Tumor Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. **All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts;
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project ...
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project ...
We are seeking an Dermatologist - Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. **All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts;
We are seeking an Dermatologist - Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. **All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts;
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Experienced Clinical Trial Manager (Oncology / Cardiovascular / Metabolic / GI)
Experienced Clinical Trial Manager (Oncology / Cardiovascular / Metabolic / GI)
Medpace
London
Competitive
Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Clinical Trial Managers with expertise in Oncology / Cardiovascular / Metabolic / GastroIntestinal indications are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. * Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred; * Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables - Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary - We provide remote flexibility only with relevant experience.
Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Clinical Trial Managers with expertise in Oncology / Cardiovascular / Metabolic / GastroIntestinal indications are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. * Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred; * Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables - Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary - We provide remote flexibility only with relevant experience.
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Strategy & CDD Industrial Products, Technology & Services - Manager / Consultant
Strategy & CDD Industrial Products, Technology & Services - Manager / Consultant
BDO
City of London (EC1)
competitive salary and package
You will join our Industrial Products, Technology & Services team as a Manager, playing a key role across Project Delivery, Business Development, Thought Leadership, and Practice Development within the Strategy & Commercial Due Diligence (CDD) practice. As a Manager in our growing Industrial Products, Technology & Services team, you will play a key role in Project Delivery, Business Development, Thought Leadership and Practice Development, working with a dedicated team of sector-focused professionals. * B2B / industrials / manufacturing Sector experience - in particular deals and growth strategy experience - Our Advisory team provide a wide variety of services that deliver value-led advice and outcomes. The team work across strategy, operations and improvement as well as at a transactional and defined project level. From technology to risk advisory, they’re experts in following through on ...
You will join our Industrial Products, Technology & Services team as a Manager, playing a key role across Project Delivery, Business Development, Thought Leadership, and Practice Development within the Strategy & Commercial Due Diligence (CDD) practice. As a Manager in our growing Industrial Products, Technology & Services team, you will play a key role in Project Delivery, Business Development, Thought Leadership and Practice Development, working with a dedicated team of sector-focused professionals. * B2B / industrials / manufacturing Sector experience - in particular deals and growth strategy experience - Our Advisory team provide a wide variety of services that deliver value-led advice and outcomes. The team work across strategy, operations and improvement as well as at a transactional and defined project level. From technology to risk advisory, they’re experts in following through on ...
NEWPREMIUM
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The Medical Director, Oncology Clinical Development will report to the Executive Medical Director, Clinical Development Lead (CDL), Oncology Clinical Development. The Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSKs clinical portfolio and will also have responsibility for engaging in medical dialogues with relevant scientific and medical leaders in order to lead clinical data generation activities. * Collaborate with other medical directors, scientists, regulatory professionals, biostatisticians, regulatory, executive staff and others in a complex matrix environment to develop and execute phase 1-3 interventional clinical trials * Ensure high quality protocol development aligned with the Clinical Development Plan ...
The Medical Director, Oncology Clinical Development will report to the Executive Medical Director, Clinical Development Lead (CDL), Oncology Clinical Development. The Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSKs clinical portfolio and will also have responsibility for engaging in medical dialogues with relevant scientific and medical leaders in order to lead clinical data generation activities. * Collaborate with other medical directors, scientists, regulatory professionals, biostatisticians, regulatory, executive staff and others in a complex matrix environment to develop and execute phase 1-3 interventional clinical trials * Ensure high quality protocol development aligned with the Clinical Development Plan ...
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A senior leadership opportunity within a global professional services organisation investing heavily in Data & AI. This is a hands-on leadership role combining Data Science, GenAI, Solution Architecture and stakeholder engagement, focused on delivering AI-powered solutions that drive measurable business impact. * Define the technical strategy for Data & AI initiatives across the business * Mentor Data Scientists and provide technical leadership across delivery teams - You'll play a key role in shaping and delivering the firm's AI roadmap, working closely with senior stakeholders to identify high-value use cases and take them from concept through to production. * Translate complex business challenges into scalable AI products and capabilities * Deliver AI use cases across document intelligence, knowledge search, workflow automation and AI assistants
A senior leadership opportunity within a global professional services organisation investing heavily in Data & AI. This is a hands-on leadership role combining Data Science, GenAI, Solution Architecture and stakeholder engagement, focused on delivering AI-powered solutions that drive measurable business impact. * Define the technical strategy for Data & AI initiatives across the business * Mentor Data Scientists and provide technical leadership across delivery teams - You'll play a key role in shaping and delivering the firm's AI roadmap, working closely with senior stakeholders to identify high-value use cases and take them from concept through to production. * Translate complex business challenges into scalable AI products and capabilities * Deliver AI use cases across document intelligence, knowledge search, workflow automation and AI assistants
FEATURED
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Senior Data Scientist
Senior Data Scientist
MASS Consultants
Little Paxton, St. Neots (PE19)
From £45,000 to £65,000 per annum DOE plus company benefits
As our Data Intelligence capability continues to grow, we're looking for a Senior Data Scientist to join the team and support the delivery of innovative data solutions across a range of exciting customer projects. As a Senior Data Scientist, you'll provide technical leadership across a variety of projects, taking ownership of delivery while helping to guide and develop less experienced team members. Based at our head office in Little Paxton, St Neots, you'll work alongside a highly skilled team of Data Scientists, Software Engineers and Technical Specialists, delivering innovative solutions for highly secure customers. You'll play a key role in delivering advanced data science capabilities, helping customers unlock value from complex datasets through analysis, visualisation, modelling, prediction and AI-driven solutions.
As our Data Intelligence capability continues to grow, we're looking for a Senior Data Scientist to join the team and support the delivery of innovative data solutions across a range of exciting customer projects. As a Senior Data Scientist, you'll provide technical leadership across a variety of projects, taking ownership of delivery while helping to guide and develop less experienced team members. Based at our head office in Little Paxton, St Neots, you'll work alongside a highly skilled team of Data Scientists, Software Engineers and Technical Specialists, delivering innovative solutions for highly secure customers. You'll play a key role in delivering advanced data science capabilities, helping customers unlock value from complex datasets through analysis, visualisation, modelling, prediction and AI-driven solutions.
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We are seeking an experienced Data Scientist with strong Data Engineering capabilities to support the Digital Screening programme. Role: Data Scientist / Engineer - You will work within a multidisciplinary Agile team, collaborating with Data Engineers, Analysts, and User-Centred Design (UCD) professionals to deliver robust, data-driven insights and scalable data solutions. * Lead exploratory data analysis (EDA) to inform dashboard design and reporting outputs * Define data requirements and determine appropriate dashboard content * Identify and mitigate data quality risks and ensure data integrity * Design, build, and maintain reusable data pipelines and datasets using Python and PySpark * Work with stakeholders to translate business needs into data solutions and insights * Solid background in exploratory data analysis and data modelling
We are seeking an experienced Data Scientist with strong Data Engineering capabilities to support the Digital Screening programme. Role: Data Scientist / Engineer - You will work within a multidisciplinary Agile team, collaborating with Data Engineers, Analysts, and User-Centred Design (UCD) professionals to deliver robust, data-driven insights and scalable data solutions. * Lead exploratory data analysis (EDA) to inform dashboard design and reporting outputs * Define data requirements and determine appropriate dashboard content * Identify and mitigate data quality risks and ensure data integrity * Design, build, and maintain reusable data pipelines and datasets using Python and PySpark * Work with stakeholders to translate business needs into data solutions and insights * Solid background in exploratory data analysis and data modelling
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Technical Manager
Technical Manager
TREVETT PROFESSIONAL SERVICES LTD
Euston, North West London (NW1), NW1 2BE
£65,000 per annum
Reporting to the Technical Director, the Technical Manager will be responsible for the management and control of all technical matters relating to plant and equipment maintenance including existing equipment, new works and future upgrade works. Trevett Services are delighted to be partnering with a leading Service Provider to source a Technical Manager for central London. Working in an iconic London building, the Technical Manager will lead on the delivery of M&E Maintenance Projects and Building Services Lifecycle Projects. My client is looking for a detail-oriented and well organised Technical Manager with excellent communication and stakeholder management skills as well as having good report writing skills. Central London £65k + benefits - About you:You will be qualified in either Electrical or Mechanical EngineeringExperience of managing multi-disciplined engineering teams
Reporting to the Technical Director, the Technical Manager will be responsible for the management and control of all technical matters relating to plant and equipment maintenance including existing equipment, new works and future upgrade works. Trevett Services are delighted to be partnering with a leading Service Provider to source a Technical Manager for central London. Working in an iconic London building, the Technical Manager will lead on the delivery of M&E Maintenance Projects and Building Services Lifecycle Projects. My client is looking for a detail-oriented and well organised Technical Manager with excellent communication and stakeholder management skills as well as having good report writing skills. Central London £65k + benefits - About you:You will be qualified in either Electrical or Mechanical EngineeringExperience of managing multi-disciplined engineering teams
Our client, a leader in the IT sector, is seeking a Technology Data Lead to oversee and deliver end-to-end data migration activities on a contract basis. If you are a skilled Technology Data Lead looking to apply your expertise in a challenging and rewarding role, we would love to hear from you. * Bachelor's degree in Information Technology, Computer Science, Information Systems, Engineering, Data Management, or a related discipline * Leading the end-to-end SAP data migration, from strategy development to execution * Defining and managing the data workstream plan and resources * Supporting profiling, cleansing, and validation of data * Managing multiple System Integrators and specialised Data Migration firms * Ensuring compliant, high-quality, and timely migration of business-critical data * Supporting testing cycles and cutover with accurate data loads
Our client, a leader in the IT sector, is seeking a Technology Data Lead to oversee and deliver end-to-end data migration activities on a contract basis. If you are a skilled Technology Data Lead looking to apply your expertise in a challenging and rewarding role, we would love to hear from you. * Bachelor's degree in Information Technology, Computer Science, Information Systems, Engineering, Data Management, or a related discipline * Leading the end-to-end SAP data migration, from strategy development to execution * Defining and managing the data workstream plan and resources * Supporting profiling, cleansing, and validation of data * Managing multiple System Integrators and specialised Data Migration firms * Ensuring compliant, high-quality, and timely migration of business-critical data * Supporting testing cycles and cutover with accurate data loads
Clinical Trial Managers with expertise in Oncology or other therapy areas are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in London, UK. * Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables * Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred; We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates. Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary
Clinical Trial Managers with expertise in Oncology or other therapy areas are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in London, UK. * Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables * Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred; We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates. Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary